ATLAS PREP BASE- chlorine dioxide teat dip liquid

Atlas Prep Base by

Drug Labeling and Warnings

Atlas Prep Base by is a Animal medication manufactured, distributed, or labeled by BOUMATIC, LLC, Knapp Manufacturing, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Claim of effectiveness.

Helps reduce the spread of organisms
which may cause Mastitis

Use Directions

NOT FOR HUMAN USE
FOR EXTERNAL USE ONLY
Do not mix with any other chemicals
other than ATLAS PREP ACTIVATOR.
In well ventilated area, combine 1 gallon
ATLAS PREP BASE and 54 gallons ATLAS
PREP ACTIVATOR, mix or stir vigorously
for at least one minute. Allow mixture to
react for 15-30 minutes prior to application.
Do not mix more product than can be
used in 1 week.

First Aid

FIRST AID:
If in eyes: Hold eye open and rinse slowly and gently with water for at least 15 minutes. Remove contact
lenses, if present and easy to do. Continue rinsing. Contact a physician immediately. If swallowed:
Rinse mouth with water. Do not give anything to an unconscious person. Do not induce vomiting. Contact
a physician immediately. If Inhaled: Move person to fresh air. Contact a physician immediately. If
on skin: Immediatly remove contaminated clothing. Rinse skin with water. Use soap if available. Wash
clothes before reuse. If irritation develops and persists, contact a physician.
Have the product container or label with you when going for treatment, calling a physician, the emergency
number listed on this label or SDS, or a poison control center.

Precautions & Hazards

Wash skin/ contaminated clothing thoroughly after handling. Wear protective gloves/
protective clothing/ eye protection/ face protection. Do not breathe vapors, mist or spray. Do not mix
with any chemicals except as directed.

General Storage

STORAGE: Store in a closed container away from sources of heat. If product becomes frozen, thaw and mix
well before use.

label

INGREDIENTS AND APPEARANCE

ATLAS PREP BASE 
chlorine dioxide teat dip liquid

Product Information
Product Type	OTC ANIMAL DRUG	Item Code (Source)	NDC: 48106-2052
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM CHLORITE (UNII: G538EBV4VF) (CHLORITE ION - UNII:Z63H374SB6)	SODIUM CHLORITE	13.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 48106-2052-1	3914 g in 1 PACKAGE
2	NDC: 48106-2052-2	19570 g in 1 PACKAGE
3	NDC: 48106-2052-3	58710 g in 1 PACKAGE
4	NDC: 48106-2052-4	117421 g in 1 PACKAGE
5	NDC: 48106-2052-5	215271 g in 1 PACKAGE
6	NDC: 48106-2052-6	1076359 g in 1 PACKAGE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/10/2023

Labeler - BOUMATIC, LLC (124727400)

Establishment
Name	Address	ID/FEI	Business Operations
BOUMATIC, LLC		124727400	api manufacture

Establishment
Name	Address	ID/FEI	Business Operations
Knapp Manufacturing, Inc.		063012827	manufacture